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Modulation of ethylene synthesis in acotyledonous soybean and wheat seedlings

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Abstract

The characteristics of ethylene production and ACC conversion in 8-day-old soybean seedlings were examined and a relationship between cytochrome P-450 activity and ethylene-forming enzyme (EFE) activity was found. An atmosphere containing 10% carbon monoxide (CO) significantly inhibited ethylene production and ACC conversion in control soybean seedlings, but had only a slight effect on soybean seedlings treated with uniconazole. Foliar application of triclopyr, a pyridine analogue of the phenoxy herbicides, significantly increased ethylene production and ACC conversion in control, but not in uniconazoletreated seedlings. Triclopyr treatment also resulted in a three-fold increase in extractable cytochrome P-450 of 5-day-old etiolated soybeans. At equimolar concentrations tetcyclacis was more effective than uniconazole in reducing shoot elongation and endogenous ethylene production. Although uniconazole and tetcyclacis did not inhibit ACC conversion in nonherbicide-treated soybean seedlings, they did prevent the observed increase in ACC-dependent EFE activity following triclopyr application. However, the rate of ACC conversion in etiolated soybean segments was sensitive to uniconazole, and tetcyclacis inhibited the rate of ACC conversion by 2.6-fold in etiolated soybean segments within 4 h after treatment. Microsomal membranes were isolated from 5-day-old naphthalic anhydride-treated etiolated wheat shoots as this tissue contains much higher cytochrome P-450 levels than soybean shoots. Optical difference spectroscopy demonstrated that ACC generated binding spectrum characteristic of a reverse-type-I cytochrome P-450 substrate when combined with reduced microsomes. In vitro conversion of ACC to ethylene by microsomal membranes was NADPH-dependent, inhibited by CO, and had an apparent Km and Vmax of 45 μM and 0.345 nl/mg protein/h, respectively. These results suggest that cytochrome P-450-mediated monooxygenase reactions may be intimately involved in the conversion of ACC to ethylene in young soybean and wheat seedlings.

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References

  • Adele P, Reichhart D, Saluan J-P, Benveniste I, Durst F (1981) Induction of cytochrome P-450 and monooxygenase activity by 2,4-D in higher plant tissue. Plant Sci Lett 22:39–46

    Article  CAS  Google Scholar 

  • Asare-Boamah NK, Hofstra G, Fletcher RA, Dumbroff EB (1986) Triademefon protects bean plants from water stress through its effects on abscisic acid. Plant Cell Physiol 27:383–390

    CAS  Google Scholar 

  • Cole DJ, Owen WJ (1987) Influence of monooxygenase inhibitors on the metabolism of the herbicides chlorotoluron and metolachlor in cell suspension cultures. Plant Sci 50:13–20

    Article  CAS  Google Scholar 

  • Donaldson RP, Luster DG (1991) Multiple forms of plant cytochromes P-450. Plant Physiol 96:669–674

    PubMed  CAS  Google Scholar 

  • Estabrook RW, Werringloer J (1978) The measurement of difference spectra: Application to the cytochromes of microsomes. In: Fleischer S, Packer L (eds) Methods in enzymology, vol. 52. Academic Press, New York, pp 212–220

    Google Scholar 

  • Fletcher RA, Hofstra G (1988) Triazoles as potential plant protectants. In: Berg D, Plempel M (eds) Sterol biosynthesis inhibitors: Pharmaceutical and Agricultural aspects. Ellis Horwood Ltd., England, pp 321–331

    Google Scholar 

  • Fonne-Pfister R, Simon A, Saluan J-P, Durst F (1988) Xenobiotic metabolism in higher plants, involvement of microsomal cytochrome P-450 in aminopyrine N-demethylation. Plant Sci 55:9–20

    Article  CAS  Google Scholar 

  • Grossmann K, Hauser C, Sauerbrey E, Fritsch H, Schmidt O, Jung J (1989) Plant growth retardants as inhibitors of ethylene production. J Plant Physiol 134:538–543

    CAS  Google Scholar 

  • Halkier BA, Moller BL (1991) Involvement of cytochrome P-450 in the biosynthesis of Dhurrin in Sorghum bicolor (L.) Moench. Plant Physiol 96:10–17

    Article  PubMed  CAS  Google Scholar 

  • Hendry G (1986) Why do plants have cytochrome P-450? Detoxification vs defence. New Phytol 102:239–247

    Article  CAS  Google Scholar 

  • Hendry G, Jones OTG (1984) Induction of cytochrome P-450 in intact mung beans. New Phytol 96:153–159

    Article  CAS  Google Scholar 

  • Jefcoate CR (1978) Measurement of substrate and inhibitor binding to microsomal cytochrome P-450 by optical-difference spectroscopy. Methods Enzymol 52:258–279

    Article  PubMed  CAS  Google Scholar 

  • Kraus TE, Murr DP, Fletcher RA (1991) Uniconazole inhibits stress-induced ethylene synthesis in wheat and soybean seedlings J Plant Growth Regul 10:157–162

    Article  Google Scholar 

  • McFadden JJ, Frear DS, Mansager ER (1989) Aryl hydroxylation of diclofop by a cytochrome P-450 dependent monooxygenase from wheat. Pestic Biochem Physiol 34:92–100

    Article  CAS  Google Scholar 

  • McFadden JJ, Gronwald JW, Eberlein CV (1990) In vitro hydroxylation of bentazon by microsomes from naphthalic anhydride-treated corn shoots. Biochem Biophys Res Commun 168:206–213

    Article  PubMed  CAS  Google Scholar 

  • Rademacher W, Fritsch H, Graebe JE, Sauter H, Jung J (1987) Tetcyclasis and triazole-type plant growth retardants: Their influence on the biosynthesis of gibberellins and other metabolic processes. Pestic Sci 21:241–252

    Article  CAS  Google Scholar 

  • Reichhart D, Saluan J-P, Benveniste I, Durst F (1980) Time course induction of cytochrome P-450, NADPH-cytochrome-(c)-reductase, and cinnamic acid hydrolysis by phenobarbital, ethanol, herbicides and manganese in higher plant microsomes. Plant Physiol 66:600–604

    PubMed  CAS  Google Scholar 

  • Sauerbrey E, Grossman K, Jung J (1988) Ethylene production by sunflower cell suspensions: Effects of plant growth retardants. Plant Physiol 87:510–513

    PubMed  CAS  Google Scholar 

  • Ververidis P, John P (1991) Complete recovery in vitro of ethylene-forming enzyme activity. Phytochemistry 30:725–727

    Article  CAS  Google Scholar 

  • West CA (1980) Hydroxylases, monooxygenases and cytochrome P-450. In: Davies DD (ed) The biochemistry of plants, vol. 2. Academic Press, London, pp 317–364

    Google Scholar 

  • Wiggins TE, Baldwin BC (1984) Binding of azole fungicides related to diclobutrazol to cytochrome P-450. Pestic Sci 15:206–209

    Article  CAS  Google Scholar 

  • Yang SF, Hoffman NE (1984) Ethylene biosynthesis and its regulation in higher plants. Ann Rev Plant Physiol 35:155–189

    CAS  Google Scholar 

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Kraus, T.E., Murr, D.P., Hofstra, G. et al. Modulation of ethylene synthesis in acotyledonous soybean and wheat seedlings. J Plant Growth Regul 11, 47–53 (1992). https://doi.org/10.1007/BF00193843

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